The following data is part of a premarket notification filed by Medtech Instruments with the FDA for Thermalgraphic Analyser.
Device ID | K894772 |
510k Number | K894772 |
Device Name: | THERMALGRAPHIC ANALYSER |
Classification | Device, Temperature Measurement, Direct Contact, Powered |
Applicant | MEDTECH INSTRUMENTS 7920 N.E. EVERETT Portland, OR 97213 |
Contact | John Megehee |
Correspondent | John Megehee MEDTECH INSTRUMENTS 7920 N.E. EVERETT Portland, OR 97213 |
Product Code | HCS |
CFR Regulation Number | 882.1570 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1989-07-26 |
Decision Date | 1989-10-03 |